# FLUOXETINE HYDROCHLORIDE
> **ANDA211051** · Abbreviated New Drug Application (Generic) · Sponsor: TEVA PHARMS USA · Approved 2018-12-03
## Drug
- **FDA Application Number:** ANDA211051
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** FLUOXETINE HYDROCHLORIDE
- **Generic name:** Fluoxetine Hydrochloride
- **Active ingredients:** FLUOXETINE HYDROCHLORIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** TEVA PHARMS USA
- **First approval:** 2018-12-03
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211051)
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